Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.

Autor: Dorval G; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France. guillaume.dorval@inserm.fr.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France. guillaume.dorval@inserm.fr., Gribouval O; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France., Martinez-Barquero V; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France., Machuca E; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France., Tête MJ; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France., Baudouin V; Department of Pediatric Nephrology, Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Paris, France., Benoit S; Department of Nephrology, University Hospital of Tours, Tours, France., Chabchoub I; Department of Pediatrics, Sfax University, Sfax, Tunisia., Champion G; Department of Pediatrics, University Hospital of Angers, Angers, France., Chauveau D; Department of Nephrology and Organ Transplantation, University Hospital Rangueil, Toulouse, France., Chehade H; Department of Pediatrics, Division of Pediatric Nephrology, Lausanne University Hospital, Lausanne, Switzerland., Chouchane C; Department of Pediatrics, Monastir University, Monastir, Tunisia., Cloarec S; Department of Nephrology, University Hospital of Tours, Tours, France., Cochat P; Department of Pediatric Nephrology, Claude-Bernard Lyon 1 University, Bron, France., Dahan K; Department of Human Genetics, Institute of Pathology and Genetics, Gosselies, Belgium., Dantal J; Nephrology and Immunology Department, University Hospital of Nantes, Nantes, France., Delmas Y; Department of Nephrology, University Hospital of Bordeaux, Bordeaux, France., Deschênes G; Department of Pediatric Nephrology, Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Paris, France., Dolhem P; Department of Pediatrics, Saint-Quentin Hospital, Saint-Quentin, France., Durand D; Department of Nephrology and Organ Transplantation, University Hospital Rangueil, Toulouse, France., Ekinci Z; Kocaeli Academy for Solidarity, Kocaeli, Turkey., El Karoui K; Department of Nephrology, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France., Fischbach M; Nephrology Dialysis Transplantation Children's Unit, University Hospital Hautepierre, Strasbourg, France., Grunfeld JP; Department of Nephrology, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France., Guigonis V; Department of Pediatrics, University Hospital of Limoges, Limoges, France., Hachicha M; Department of Pediatrics, Sfax University, Sfax, Tunisia., Hogan J; Department of Pediatric Nephrology, Assistance Publique-Hôpitaux de Paris, Armand Trousseau Hospital, Paris, France., Hourmant M; Nephrology and Immunology Department, University Hospital of Nantes, Nantes, France., Hummel A; Department of Nephrology, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France., Kamar N; Department of Nephrology and Organ Transplantation, University Hospital Rangueil, Toulouse, France., Krummel T; Department of Nephrology, University Hospital Hautepierre, Strasbourg, France., Lacombe D; Department of Genetics, University Hospital of Bordeaux, Bordeaux, France., Llanas B; Department of Pediatrics, University Hospital of Bordeaux, Bordeaux, France., Mesnard L; Department of Nephrology and Dialysis, Assistance Publique-Hôpitaux de Paris, Tenon Hospital, Paris, France.; Sorbonne University, UPMC University Paris 06, Paris, France.; INSERM, UMR_S 1155, 75020, Paris, France., Mohsin N; College of Medicine, Sultan Qaboos University, Muscat, Oman., Niaudet P; Department of Pediatric Nephrology, Centre de référence du syndrome néphrotique idiopathique de l'enfant et l'adulte, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Centre de Référence Syndrome Néphrotique Idiopathique de l'enfant et de l'adulte, Paris, France., Nivet H; Department of Nephrology, University Hospital of Tours, Tours, France., Parvex P; Department of Pediatrics, Division of Pediatric Nephrology, Geneva University Hospital, Geneva, Switzerland., Pietrement C; Departement of Pediatrics, Nephrology Unit, University Hospital of Reims, Reims, France.; Faculty of Medicine, Laboratory of Biochemistry and Molecular Biology, UMR, CNRS/URCA n°7369, University of Champagne-Ardenne, Reims, France., de Pontual L; Department of Pediatrics, Assistance Publique-Hôpitaux de Paris, Jean Verdier Hospital, Bondy, France., Noble CP; Department of Nephrology and Transplantation, University Hospital of Lyon, Lyon, France., Ribes D; Department of Nephrology and Organ Transplantation, University Hospital Rangueil, Toulouse, France., Ronco P; Department of Nephrology and Dialysis, Assistance Publique-Hôpitaux de Paris, Tenon Hospital, Paris, France.; Sorbonne University, UPMC University Paris 06, Paris, France.; INSERM, UMR_S 1155, 75020, Paris, France., Rondeau E; Department of Nephrology and Dialysis, Assistance Publique-Hôpitaux de Paris, Tenon Hospital, Paris, France., Sallee M; Department of Nephrology and Kidney Transplantation, The Conception Hospital, Marseille, France., Tsimaratos M; Department of Multidisciplinary Pediatrics Timone, Assistance Publique Hôpitaux de Marseille, Aix-Marseille University, Marseille, France., Ulinski T; Department of Pediatric Nephrology, Assistance Publique-Hôpitaux de Paris, Armand Trousseau Hospital, Paris, France., Salomon R; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Department of Pediatric Nephrology, Centre de référence du syndrome néphrotique idiopathique de l'enfant et l'adulte, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Centre de Référence Syndrome Néphrotique Idiopathique de l'enfant et de l'adulte, Paris, France., Antignac C; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Centre de Référence Syndrome Néphrotique Idiopathique de l'enfant et de l'adulte, Paris, France.; Department of Genetics, Assistance Publique-Hôpitaux de Paris, Necker-Enfants malades Hospital, Paris, France., Boyer O; INSERM UMR1163, Laboratory of Hereditary Kidney Diseases, Imagine Institute, 24 Boulevard du Montparnasse, 75015, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France.; Department of Pediatric Nephrology, Centre de référence du syndrome néphrotique idiopathique de l'enfant et l'adulte, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France.; Centre de Référence Syndrome Néphrotique Idiopathique de l'enfant et de l'adulte, Paris, France.

Publikováno v: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2018 Mar; Vol. 33 (3), pp. 473-483. Date of Electronic Publication: 2017 Oct 23.

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations.

Autor: Temme J; Department of Nephrology and Rheumatology, University Medical Center Göttingen, Göttingen, Germany., Peters F, Lange K, Pirson Y, Heidet L, Torra R, Grunfeld JP, Weber M, Licht C, Müller GA, Gross O

Publikováno v: Kidney international [Kidney Int] 2012 Apr; Vol. 81 (8), pp. 779-83. Date of Electronic Publication: 2012 Jan 11.

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.

Autor: Boyer O; INSERM U983, Tour Lavoisier, 6 étage, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75015 Paris, France., Benoit G, Gribouval O, Nevo F, Tête MJ, Dantal J, Gilbert-Dussardier B, Touchard G, Karras A, Presne C, Grunfeld JP, Legendre C, Joly D, Rieu P, Mohsin N, Hannedouche T, Moal V, Gubler MC, Broutin I, Mollet G, Antignac C

Publikováno v: Journal of the American Society of Nephrology : JASN [J Am Soc Nephrol] 2011 Feb; Vol. 22 (2), pp. 239-45. Date of Electronic Publication: 2011 Jan 21.

Risk scores for predicting outcomes in patients with type 2 diabetes and nephropathy: the RENAAL study.

Autor: Keane WF; Merck & Co., Inc., Whitehouse Station, New Jersey, USA. williamf_keane@merck.com, Zhang Z, Lyle PA, Cooper ME, de Zeeuw D, Grunfeld JP, Lash JP, McGill JB, Mitch WE, Remuzzi G, Shahinfar S, Snapinn SM, Toto R, Brenner BM

Publikováno v: Clinical journal of the American Society of Nephrology : CJASN [Clin J Am Soc Nephrol] 2006 Jul; Vol. 1 (4), pp. 761-7. Date of Electronic Publication: 2006 May 17.

Recovery of acute renal failure and nephrotic syndrome following autologous stem cell transplantation for primary (AL) amyloidosis.

Autor: Snanoudj R; Nephrology Department, Hôpital Necker, Assistance Publique Hôpitaux de Paris, France. rsnanoudj@aol.com, Mamzer-Bruneel MF, Hermine O, Grunfeld JP, Chauveau D

Publikováno v: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2003 Oct; Vol. 18 (10), pp. 2175-7.